EP1501774B9 - Mehrfach ungesättigte, geradkettige aldehyde und deren derivate mit anti-radikalwirkung - Google Patents

Mehrfach ungesättigte, geradkettige aldehyde und deren derivate mit anti-radikalwirkung Download PDF

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EP1501774B9
EP1501774B9 EP03749867A EP03749867A EP1501774B9 EP 1501774 B9 EP1501774 B9 EP 1501774B9 EP 03749867 A EP03749867 A EP 03749867A EP 03749867 A EP03749867 A EP 03749867A EP 1501774 B9 EP1501774 B9 EP 1501774B9
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Prior art keywords
aldehydes
derivatives
compounds
formula
hours
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EP1501774B1 (de
EP1501774A1 (de
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Riccardo Stradi
Aldo Bertelli
Elena Pini
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Giuliani SpA
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/11—Aldehydes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
    • A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4986—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with sulfur as the only hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/738—Cyclodextrins
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A61P39/06—Free radical scavengers or antioxidants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/08—Anti-ageing preparations
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/02—Acyclic alcohols with carbon-to-carbon double bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/21—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/24—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds

Definitions

  • This invention relates to polyunsaturated linear aldehydes and their derivatives with anti-radical activity.
  • this invention relates to the use of polyunsaturated linear aldehydes which can be extracted from parrot feathers and tissues or prepared synthetically, and of derivatives of said aldehydes such as fatty esters of alcohols obtained by reduction of the aldehyde group, or derivatives of inclusion of said aldehydes in cyclodextrins, as antioxidant and anti-inflammatory agents.
  • This invention also relates to novel derivatives of said aldehydes, such as some alcohols obtained by reduction of the aldehyde group, fatty esters of alcohols and derivatives of inclusion of aldehydes in cyclodextrins.
  • Said polyunsaturated aldehydes and the derivatives thereof will hereafter be generically referred to as "parrodienes”.
  • parrodienes of the invention possess antioxidant and anti-inflammatory activity and are therefore useful in preventing the damage caused by free radicals, and in particular in the prevention and treatment of, and the prevention of alterations caused by skin ageing.
  • Known examples are polyunsaturated fatty acids extracted from fish (1, 2, 3), glycosaminoglycans extracted from the cartilage of animals such as the shark (3, 4, 5, 6, 8), glycoproteins such as lactoferrin extracted from milk or colostrum (9, 10), and lipid extracts of molluscs such as oysters (11, 12).
  • Lutein, zeaxanthin and beta-cryptoxanthins are carotenoids frequently found in foods (berries, fruit, seeds, flowers and insects), which can be absorbed by tissues and feathers with no metabolic modifications to their structure, whereas other compounds, such as picofulvins, are the result of molecular modification (13, 14, 15, 16).
  • the psittacofulvins or the mixture of parrodienes are the result of metabolic changes typical of various species of parrot ( Poicephalus rufiventris, Ara macao, Ara manilata, Ara ararauna, Psittacus erithacus, Aratinga canicularis, Aratinga acuticaudata, Psittacula krameri , etc.).
  • the parrodienes according to the invention have an antioxidant activity and in general a protective effect against the free radicals, which may explain the exceptional longevity of these animals (they can live for up to 100 years), their learning ability, and above all their lack of diseases, especially tumours.
  • reaction mixture is cooled in an ice bath and added with 600 ml of ethyl ether, still under magnetic stirring.
  • brown precipitate formed is filtered and recrystallized from toluene: 120 mg of 2,4,6,8,10,12,14-hexadecaheptaenal is obtained.
  • the red ether solution is extracted with 200 x 5 ml of distilled water to wash away the unreacted surplus crotonaldehyde; the organic phase is dried over sodium sulphate and evaporated under pressure (30 mmHg).
  • the brownish-red residue is taken up with 30 ml of 80% methanol and left in the refrigerator overnight at 3°C. 2,4,6,8,10-dodecapentaenal is thus separated by precipitation, and is recrystallized from isopropanol (2.5 g).
  • acetaldehyde and 140 ml of crotonaldehyde are placed in a 1-litre flask, and kept under magnetic stirring for 30 minutes under nitrogen flow.
  • 2 ml of piperidine and 1.4 ml of acetic acid are slowly dropped therein, and the mixture is left under magnetic stirring in a nitrogen atmosphere for 18 hours.
  • 500 ml of ethyl ether are added to the red solution; the precipitate is filtered, then recrystallized from toluene.
  • the precipitate obtained is 2,4,6,8,10,12,14-hexadecaheptaenal (140 mg), whereas 2,4,6,8,10,12-tetradecahexaenal (25 mg) is isolated from the evaporated toluene phase.
  • the residue obtained from evaporation of the organic phase is subjected to fractional distillation: unreacted crotonaldehyde is obtained at 21°C (30 mmHg), 2,4-hexadienal at 26°C (3 mmHg, 5.2 g) and 2,4,6-octatrienal at 55-60°C (3 mmHg).
  • the residue is taken up with 30 ml of 80% methanol; 2,4,6,8-decatetraenal is separated by precipitation at -20°C and then filtered and recrystallized from hexane (420 mg).
  • esters described in the table below were prepared in accordance with the procedure described above.
  • No. NAME Reaction time % yield 2 2,4-hexadienyl palmitate 4 hours 94 3 2,4,6,8-decatetraenyl palmitate 24 hours 86 4 2,4,6,8,10-dodecapentaenyl palmitate 24 hours 84 5 2,4,6,8,10,12-tetradecahexaenyl palmitate 24 hours 60 6 2,4,6,8,10,12,14-hexadecaheptaenyl palmitate 24 hours 40
  • PC-12 phaeochromocytoma cells
  • PC-12 phaeochromocytoma cells
  • CCl 4 The lipoperoxidative and toxic effect induced by CCl 4 (100 mg/L -1 ) was evaluated on rat hepatocytes isolated according to the technique described by Segler ( Segler P.O., Methods Cell. Biol. Chem., 264, 4747, 1989 ).
  • CCl 4 is known to cause lipoperoxidation of the cell membranes which can lead to cell necrosis ( Slater T.F., Philos Trans. R. Soc. Lond. (Biol) 311, 633, 1985 ; Berger M.L., Hepatology, 6, 36, 1996 ; Tribble D.L., Hepatology, 7, 377, 1987 ).
  • the damage to the cell membrane caused by CCl 4 and the protective effect performed were measured by assaying alanine aminotransferase (AlaAT) and aspartate aminotransferase (AspoAT) on the supernatant liquid of the cell culture (Auto-biochemistry Assay System-Beeckman 700-Encore-2).
  • the histological tests also demonstrated the protection provided by parrodin.
  • Red blood cells were extracted from the venous blood of healthy volunteers; after centrifugation and washing in saline buffered with PBS phosphates (0.15M, pH 7.4) they were diluted with 10 cc of a solution containing 10 -3 M of PBS-azide, and the haemoglobin concentration was measured with Drabkin's reagent. Lipid peroxidation was induced by exposing a cell expansion contained in 5 cc of PBS-azide with a final haemoglobin concentration of 3.75 mg/ml to hydrogen peroxide (20 mM of hydrogen peroxide per ampoule containing 5 cc of cell suspension) and incubating them at 37° for one hour.
  • Peroxidation was determined after one hour according to the Stocks and Dormandy method ( Stocks J., Dormandy T.L., Brit. J. Haematology, 29, 95, 1971 ) that measures the formation of malonaldehyde which, in combination with thiobarbituric acid (TBA), forms a coloured chromogen with absorbance at 532 nm ( Bird R.P., Methods Enzymol, 105, 299, 1984 ).
  • the antilipoperoxidative activity of parrodin was evaluated by introducing it into tubes containing the erythrocyte suspension at the dose of 100 mcg/ml.
  • Platelet aggregation was determined on platelet-rich plasma (PRP); the number of platelets was counted with a CH58 oH platelet counter (Delcan) and made up to 300,000 platelets/ml with platelet-poor plasma (PPP).
  • PRP platelet-rich plasma
  • Delcan CH58 oH platelet counter
  • PPP platelet-poor plasma
  • Platelet aggregation was induced by adding collagen (2.5 ng/ml) and evaluated photometrically with an aggregometer according to the technique described by Born ( Born G.V.R., Nature 194, 927, 1962 ).
  • UV-induced erythema was caused by applying a UV lamp (Hanoivna Kramager) to the ear of a guinea pig for 30 sec; the lamp transmitted rays with a wavelength of 200 to 400 mm, which consequently included UV-B, UV-C and UV-A rays, through a special filter.
  • a UV lamp Hanoivna Kramager
  • the set of tests performed indicates that the polyunsaturated linear compounds according to the invention possess the biological characteristics common to carotenoids of plant or other origin, and demonstrate a particular protective activity against hydroperoxides and free radicals.
  • They consequently seem likely to be particularly useful in the prevention and treatment of all the organic changes caused by the activation of free radical production. They can be used as diet supplements, medicaments or cosmetics in the prevention or treatment of various disorders associated with tissue aging. In cosmetology in particular, they can be used to treat lesions caused by ultraviolet rays and skin aging processes, inflammatory or degenerative reactions.
  • the compounds according to the invention can be employed alone or in association with one another, or in association with other carotenoids or compounds with a similar, complementary activity, such as organic or inorganic antioxidants, vitamins, aminoacids, enzymes or other products with nutritional characteristics or characteristics available in cosmetology.
  • the compounds according to the invention may be formulated in the form of ointments, creams or lotions for topical cosmetic cutaneous use.
  • formulations will be prepared according to conventional techniques, using excipients suitable for pharmaceutical or cosmetological use.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Birds (AREA)
  • Emergency Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nanotechnology (AREA)
  • Dermatology (AREA)
  • Molecular Biology (AREA)
  • Toxicology (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Medical Informatics (AREA)
  • Gerontology & Geriatric Medicine (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biochemistry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Plant Substances (AREA)

Claims (6)

  1. Verwendung von Verbindungen der allgemeinen Formel (I) :
    Figure imgb0007
     worin
    n = 2 - 7,
    R = CHO, CH2OH, CH2O-C-(O)R', worin -CO-R' für den Rest einer Fettsäure mit 12-22 Kohlenstoffatomen steht,
    alleine oder in einem Gemisch davon topisch aufträgt, für die Herstellung einer topischen Zusammensetzung zur Behandlung von durch ultraviolette Strahlen und Alterungsprozesse verursachten Hautschäden.
  2. 2,4,6,8,10,12-Tetradecahexaenol der Formel (I), worin n = 6 und R = CH2OH.
  3. 2,4,6,8,10,12,14-Hexadecaheptaenol der Formel (I), worin n = 7 und R = CH2OH.
  4. Verbindungen der allgemeinen Formel (I), worin n = 2, 3, 4, 5 oder 6 und R = CH2O-CO-R', worin -CO-R' für den Rest von Palmitinsäure steht.
  5. Einschlußverbindungen von Verbindungen der Formel (I) in Cyclodextrinen
    Figure imgb0008
     worin
    n = 2 - 7 und R = CHO.
  6. Verwendung von Verbindungen der Formel (I)
    Figure imgb0009
     für die Herstellung einer topischen Zusammensetzung, die eine Antioxidations- und entzündungshemmende Aktvität hat.
EP03749867A 2002-05-07 2003-05-06 Mehrfach ungesättigte, geradkettige aldehyde und deren derivate mit anti-radikalwirkung Expired - Lifetime EP1501774B9 (de)

Priority Applications (2)

Application Number Priority Date Filing Date Title
SI200331667T SI1501774T1 (sl) 2002-05-07 2003-05-06 Polinenasiäśeni ravnoveriĺ˝ni aldehidi in njihovi derivati s protiradikalno aktivnostjo
CY20091101096T CY1109512T1 (el) 2002-05-07 2009-10-21 Πολυακορεστες γραμμικες αλδευδες και τα παραγωγα τους με δραση εναντιον των ελευθερων ριζων

Applications Claiming Priority (3)

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ITMI20020960 2002-05-07
IT2002MI000960A ITMI20020960A1 (it) 2002-05-07 2002-05-07 Aldeidi lineari poliinsature e loro derivati ad attivita' antiradicalica e antitumorale
PCT/EP2003/004720 WO2003095403A1 (en) 2002-05-07 2003-05-06 Polyunsaturated linear aldehydes and their derivatives with anti-radical and anti-tumoral activity

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EP1501774A1 EP1501774A1 (de) 2005-02-02
EP1501774B1 EP1501774B1 (de) 2009-08-12
EP1501774B9 true EP1501774B9 (de) 2010-02-24

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US (1) US20050175555A1 (de)
EP (1) EP1501774B9 (de)
AT (1) ATE439338T1 (de)
AU (1) AU2003232722A1 (de)
CY (1) CY1109512T1 (de)
DE (1) DE60328769D1 (de)
DK (1) DK1501774T3 (de)
ES (1) ES2329890T3 (de)
IT (1) ITMI20020960A1 (de)
PT (1) PT1501774E (de)
SI (1) SI1501774T1 (de)
WO (1) WO2003095403A1 (de)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0111872D0 (en) * 2001-05-15 2001-07-04 Northwick Park Inst For Medica Therapeutic agents and methods
US7968605B2 (en) * 2002-02-04 2011-06-28 ALFAMA—Investigação e Desenvolvimento de Produtos Farmacêuticos, Lda. Methods for treating inflammatory disease by administering aldehydes and derivatives thereof
JP2005519928A (ja) * 2002-02-04 2005-07-07 ハース，ベルナー Ｃｏ放出能力を有する化合物の投与によって哺乳動物を治療する方法と、ｃｏ放出能力を有する化合物ならびにその医薬組成物
US20080026984A1 (en) * 2002-02-04 2008-01-31 Alfama - Investigacao E Desenvolvimento De Productos Farmaceuticos Lda Methods for treating inflammatory disease by administering aldehydes and derivatives thereof
GB2395432B (en) * 2002-11-20 2005-09-14 Northwick Park Inst For Medica Therapeutic delivery of carbon monoxide to extracorporeal and isolated organs
US20070207217A1 (en) * 2003-02-03 2007-09-06 Alfama - Investigacao E Desenvolvimento De Productos Farmaceuticos Lda Method for treating a mammal by administration of a compound having the ability to release CO
GB0601394D0 (en) 2006-01-24 2006-03-01 Hemocorm Ltd Therapeutic delivery of carbon monoxide
GB0605900D0 (en) * 2006-03-23 2006-05-03 Lipigen As Modulators of nuclear receptors
US9078852B2 (en) * 2008-02-29 2015-07-14 The Brigham And Women's Hospital, Inc. Retinaldehyde in the treatment of obesity, diabetes and other conditions
IT1394921B1 (it) * 2008-11-10 2012-07-27 Giuliani Spa Uso di composti come principi attivi per migliorare l'azione di riparazione cellulare dell'epidermide umana, e composizioni farmaceutiche e cosmetiche che li contengono
IT1391663B1 (it) * 2008-11-10 2012-01-17 Giuliani Spa Uso di composti atti ad inibire l' attivita' dell'enzima 5alfa-reduttasi e composizioni farmaceutiche e cosmetiche che li contengono
EP2241543A1 (de) 2009-04-17 2010-10-20 Giuliani S.p.A. Verfahren zur Herstellung von 2,4,6-Octatrien-1-säure und 2,4,6-Octatrien-1-ol
IT1401289B1 (it) 2010-04-22 2013-07-18 Giuliani Spa Composti dotati di attivita' antiossidante nei confronti dei radicali liberi, e composizioni farmaceutiche e cosmetiche che li contengono
EP2407163A1 (de) * 2010-07-16 2012-01-18 Giuliani S.p.A. Verbindungen mit einer Hautpigmentierungsaktivität und pharmazeutische oder kosmetische Zusammensetzungen damit
ES2656237T3 (es) 2011-04-19 2018-02-26 Alfama, Inc. Moléculas liberadoras de monóxido de carbono y usos de las mismas
EP2734235B1 (de) 2011-07-21 2017-03-22 Alfama, Inc. Kohlenmonoxidfreisetzende rutheniummoleküle und ihre verwendungen
JP2023142625A (ja) * 2022-03-25 2023-10-05 株式会社ダイセル クロトンアルデヒドの製造方法
CN117229132B (zh) * 2023-11-10 2024-02-20 济南悟通生物科技有限公司 一种反式-2,4-壬二烯醛的合成方法

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US3679792A (en) * 1969-09-05 1972-07-25 Wrigley W M Jun Co Dialdehyde-containing anti-caries chewing gum compositions
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WO2003095403A1 (en) 2003-11-20
ATE439338T1 (de) 2009-08-15
ITMI20020960A1 (it) 2003-11-07
US20050175555A1 (en) 2005-08-11
EP1501774B1 (de) 2009-08-12
EP1501774A1 (de) 2005-02-02
ITMI20020960A0 (it) 2002-05-07
SI1501774T1 (sl) 2009-12-31
DK1501774T3 (da) 2009-12-14
DE60328769D1 (de) 2009-09-24
CY1109512T1 (el) 2014-08-13
PT1501774E (pt) 2009-10-15
AU2003232722A1 (en) 2003-11-11

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